Palate retainer with attached nasopharyngeal airway extender for use in the treatment of obstructive sleep apnea

ABSTRACT

A medical appliance for the treatment of obstructive sleep apnea in a patient, the appliance comprising: a securing device configured to be removably affixed to the patient&#39;s jaw; and a biasing member which is insertable behind the soft palate and/or the base of the patient&#39;s tongue, thereby providing for the flow of air in the nasopharyngeal airway; wherein the securing device is connected to the biasing member to allow insertion and/or removal of the biasing member from the nasopharyngeal airway.

BACKGROUND 1. Field

The present disclosure relates generally to the use of an interoralappliance, such as a palate retainer configured with a nasopharyngealextension. The nasopharyngeal extension is a tube or airway extenderthat fits behind the soft palate with the lumen large enough to allowadequate air to pass behind the soft palate in the nasopharynx. It mayalso be extended to pass upwards behind the soft palate and downwardsbehind the base of tongue.

2. Discussion of the Background Art

The sleep apnea syndrome, and in particular obstructive sleep apnea,afflicts an estimated 2-5% of the general population and is due toepisodic upper airway obstruction during sleep. Those afflicted withobstructive sleep apnea experience sleep fragmentation and intermittent,complete or nearly complete cessation of ventilation during sleep withpotentially severe degrees of oxy hemoglobin unsaturation. Thesefeatures may be translated clinically into debilitating daytimesleepiness, cardiac disrhythmias, pulmonary-artery hypertension,congestive heart failure and cognitive dysfunction. Other problemsrelated to sleep apnea include carbon dioxide retention duringwakefulness as well as during sleep, and continuous reduced arterialoxygen tension. Hypersomnolent sleep apnea patients may be at risk forexcessive mortality from these factors as well as from an elevated riskfor accidents such as while driving or operating other potentiallydangerous equipment.

Although details of the pathogenesis of upper airway obstruction insleep apnea patients have not been fully defined, it is generallyaccepted that the mechanism includes either anatomic or functionalabnormalities of the upper airway which result in increased air flowresistance. Such abnormalities may include narrowing of the upper airwaydue to suction forces evolved during inspiration, the effect of gravitypulling the tongue back to appose the pharyngeal wall, and/orinsufficient muscle tone in the upper airway dilator muscles. It hasalso been hypothesized that a mechanism responsible for the knownassociation between obesity and sleep apnea is excessive soft tissue inthe anterior and lateral neck which applies sufficient pressure oninternal structures to narrow the airway.

One theory of the cause for the sleep disturbance is the relaxation ofthe tongue and pharyngeal walls to varying degrees during the severalstages of sleep. When fully awake, these tissues have normal tone as airpasses in and out of the lungs during respiration. However, duringsleep, the musculature supporting these tissues relaxes. As air isinspired, the tongue and posterior walls of the pharynx collapse,causing snoring or more seriously causing partial or completeobstruction of the airway.

Obstructive sleep apnea occurs due to a collapse of soft tissue withinthe upper airway during sleep. The ongoing force of inspiration servesto generate increasingly negative pressure within the pharynx, causingfurther collapse. The lack of respiration results in inadequate bloodoxygenation, and rising carbon dioxide levels. The cardiovascularresponse produces an increase in the blood pressure and pulse, andcardiac arrhythmias often occur. The carbon dioxide increase and oxygendesaturation triggers a transition to a lighter sleep stage, usuallywithout wakefulness. This transition brings a return to tonicity of themuscles of the upper airway, allowing normal breathing to resume. Theperson then returns to deeper stages of sleep and the process isrepeated. The disease is quantified in terms of respiratory disturbancesper hour. Mild disease begins at 2-3 APNEAS per hour, and it is notuncommon to find patients with indices of about one hundred or more.

Not surprisingly, sleep is extremely fragmented and of poor quality inpersons suffering from sleep apnea. As a result, such persons typicallyfeel tired upon wakening and may fall asleep at inappropriate timesduring the day. All aspects of quality of life, from physical andemotional health, to social functioning are impaired by obstructivesleep apnea.

Surgical Treatments

The treatment of sleep apnea has included such surgical interventions asUvulopalatopharyngoplasty (UPPP) gastric surgery for obesity, andmaxillo-facial reconstruction. Another mode of surgical interventionused in the treatment of sleep apnea is tracheostomy. These treatmentsconstitute major undertakings with considerable risk of post-operativemortality. In UPPP, any remaining tonsil tissue and a portion of softpalate is removed. The procedure often increases the nasopharyngealairway. However, UPPP does not always fix a sagging soft palate nor doesit address apnea caused by obstructions caused by the base of the tonguebeing deeper in the oropharynx part of the airway. These surgicaltechniques are extremely invasive, requiring general anesthesia, and aprolonged, painful recovery.

LAUP, or Laser-Assisted Uvulopalatoplasty, is a modification of theabove-mentioned technique, but has had mixed success and cannot solveobstructions in the foropharynx part of the airway or sleep apnea.

Radio frequency tissue ablation (RFTA) with the trade name“Somnoplasty,” has been used to shrink the soft palate, uvula and reducetongue volume in the treatment of snoring and obstructive sleep apnea.Somnoplasty utilizes a radiofrequency tool that generates heat to createcoagulative lesions at specific locations within the upper airway. Thelesions created by the procedure are naturally resorbed in approximatelythree to eight weeks, reducing excess tissue volume and increasing theairway opening. Like UPPP and LAUP, more than one session is typicallyrequired, and other surgeries may still be necessary in moderate tosevere cases, and there are occasional problems with morbidity.

Another area of surgical interest lies in techniques designed to pullthe tongue anteriorly. The most recent such surgical system designed totreat snoring (as well as obstructive sleep apnea) was approved by theFDA in February 1998. Known as the tongue suspension procedure (with thetrade name Repose), it is intended to pull the tongue forward, therebykeeping the tongue from falling into the airway during sleep. The systemutilizes a bone screw inserted into the mandible. The screw attaches toa non-absorbable suture which travels the length of the tongue and back.Similarly, the hyoid bone can be drawn anteriorly with two distinctscrews, also attached to the mandible.

Techniques have also been developed for treating, specifically, thecondition of snoring. Conrad et al., U.S. Pat. No. 6,250,307 discloses amethod for treating snoring of a patient, which includes embedding animplant into a soft palate of a patient in order to alter a dynamicresponse of a soft palate to airflow. The methods of Conrad et al. arespecifically designed to reduce the audibility of snoring but do notaddress the more serious condition of sleep apnea.

These conventional treatments continue to suffer poor cure rates. Thefailures lie in their inability to maintain patency in the retropalatalregion and retroglossal region (the caudal margin of the soft palate tothe base of the epiglottis). The poor success rates combined with highmorbidity from some of the surgical interventions, contribute to anongoing need for more effective treatments for sleep apnea and/orsnoring.

Pharmacological Treatments

Pharmacological therapy, aimed at stimulating upper airway muscle toreduce apneas, also have, in general, been disappointing. In addition,side effects from the pharmacological agents that have been used arefrequent. Thus, medical practitioners continue to seek non-invasivemodes of treatment for sleep apnea with high success rates and highpatient compliance including, for example in cases of minor to moderatesleep apnea relating to obesity, weight loss through a regimen ofexercise and regulated diet.

Other Non-surgical Treatments

Other non-surgical treatments for sleep apnea include the use of oraldevices and appliances that work to prevent the tongue from fallingbackwards or help reduce the collapse of the soft palate. Still othertreatments involve the use of retainers that push the lower jaw forward,thereby pulling the tongue slightly forward and, in some cases, helpingelevate the soft palate. Also, there are devices that pull on the tongueto keep it forward during sleep. These current oral devices typically donot create a significant improvement except in mild to moderate casesand can be associated with movement of the teeth over time of problemswith the temporamandibular joint.

Recent work in the treatment of sleep apnea has included the use ofcontinuous positive airway pressure (CPAP) to maintain the airway of thepatient in a continuously open state during sleep. For example, U.S.Pat. No. 4,655,213 and Australian patent AU-B-83901/82 both disclosesleep apnea treatments based on continuous positive airway pressureapplied within the airway of the patient.

Also of interest is U.S. Pat. No. 4,773,411 which discloses a method andapparatus for ventilatory treatment characterized as airway pressurerelease ventilation and which provides a substantially constant elevatedairway pressure with periodic short term reductions of the elevatedairway pressure to a pressure magnitude no less than ambient atmosphericpressure.

Although CPAP has been found to be very effective and well accepted, itsuffers from some of the same limitations, although to a lesser degree,as do the surgical options; specifically, a significant proportion ofsleep apnea patients do not tolerate CPAP well. Thus, development ofother viable non-invasive therapies has been a continuing objective inthe art.

Still others have attempted to solve sleep apnea disorders usingintraorally fitted appliances, including U.S. Pat. Nos. 4,981,437 and4,932,867, that disclose a method and apparatus for constructingdentures, which are useful, for example, in treating breathingdisorders. U.S. Pat. No. 4,386,405 discloses a device for measuring thelocation, attitude, or change of location of a patient's lower jaw. U.S.Pat. No. 4,859,181 relates to optical measurement of jaw movement. U.S.Pat. Nos. 3,998,209 and 4,220,142 disclose conditioning systems for usein a program of behavior modification to eliminate snoring, while U.S.Pat. No. 4,976,618 relates to treatment of temporomandibular jointdysfunction and bruxism. U.S. Pat. No. 3,297,021 discloses an intraoralstrain gauge and telemetering of information from an intraoral locationto an outside indicator.

The following U.S. patents purport to relate to tongue positioningand/or retaining apparatus: U.S. Pat. Nos. 5,154,184, 5,092,346,5,046,512, 4,676,240, 4,169,473, 4,304,227 and 4,593,686. Other patentsaddressing the matter of tongue positioning include the following: U.S.Pat. Nos. 5,649,540, 5,465,734, 5,373,859, 5,052,409, 4,715,368,4,196,724, 3,884,226, 3,312,216 and 3,132,647, as well as EuropeanPatent 0182387 and British Patent 874,480. The following patents purportto relate to chin straps or similar apparatus intended to hold the jawclosed: U.S. Pat. Nos. 3,312,217, 2,711,730 and 1,990,411.

Other patents relate to apparatus for interaction with the soft palatein the user's oral cavity. These include U.S. Pat. Nos. 4,669,459 and5,316,020, German patent no. DE 40 26 602 and European patent no. EP0264516. Other patents of general interest include U.S. Pat. Nos.5,056,534 and 2,705,006, German patent nos. 65194 and 2320501, and PCTpublication no. WO 92/05752 and European patent application no. 0 487469 A1.

While the above-identified conventional devices and surgical techniquesare purported to treat upper airway instability, such as OSA or snoring,they are successful, if at all, in only a limited pool of patients orunder limited circumstances. Therefore, there remains a relatively largenumber of patients whose airway disorder is believed to be treatableusing an intraoral appliance, yet conventional appliances areineffective, overly burdensome, uncomfortable, or any combinationthereof.

The present disclosure overcomes the aforementioned disadvantages of theprior art by using a novel palate retainer with a nasopharyngealextension, wherein the nasopharyngeal extension fits behind the softpalate with a tube that has a lumen large enough to allow for thepassage of air in the nasopharynx.

The present disclosure also provides many additional advantages, whichshall become apparent as described below.

SUMMARY

The present disclosure pertains to methods and/or medical appliances ordevices which are preferably attached to the upper or lower jaws, forentering the mouth horizontally with a compressed device, in a way thatminimizes triggering the gag reflex of a patient, and then having partof the device (e.g., a tube or two tubes on the side or some other kindof expander for the airway) go vertical (i.e. in a superiordirection)—up behind the soft palate and/or down (i.e. in an inferiordirection) behind part of the tongue. It is preferable, to provide adevice which allows for further expansion of the tube or tubes once inplace in the airway, in a way that still allows for swallowing.

A novel palate retainer with a nasopharyngeal extension, that fitsbehind the soft palate with a tube or other airway extender that has alumen large enough to allow for the passage of air in the nasopharynxand behind the tongue. In particular, the palate retainer is designed tobe secured to the upper palate of a patient's jaw, similar to a retainerdevice, so as to position the nasopharyngeal extension, e.g., a tube orother airway expander, behind the soft palate. This tube or spacer isdesigned to protrude from the posterior end of the palatal retainer.This tube is typically connected to the retainer by a connecting collarportion which slips underneath the soft palate and the tube ends upbehind the soft palate. The tube is preferably relatively short inlength during placement, but could be expanded after placement. Thisappliance would physically splint the palate and the tongue and preventthe palate from falling back, help stabilize the tongue and at the sametime, provide a rigid airway in the retropalatal and retrolinqual spacethat cannot collapse.

The tube can have a round cross-section or be flatter and wider, similarto a wide soft palate, as that shape could be more tolerable for thepatient, particularly during swallowing. Alternatively, the tube canhave a section that is a compressed flexible tube, with several hardplastic rings which help prevent collapse of the flexible tube. Thistube configuration can attached to the top of a rigid tube and, once inplace behind the soft palate, can be released to spring upwards ordownwards (if attached to the bottom of the rigid tube, as needed. It ispreferably, that the tube be partially flexible to allow for extractionafter use. The bottom tube could also be a firm tube that fits withinthe attached tube and then falls downward from gravity or is has a smallspring that, when released, pushes this inner section of the tubedownwards. If the bottom extension is a firm tube, then it is preferablethat the tube be flexible where it joins the firm tube on the retainer,so as to allow for extraction by bending during extraction, after it hasbeen expanded downward in place behind the base of tongue.

Yet another embodiment comprises two tubes on either side, held behindthe soft palate.

Still another embodiment involves the attached tube or airway expanderwhich has a compressed diameter which expands once in place—so as toallow an easier entry in some patients.

Furthermore, the present disclosure is a palate retainer having only oneribbon-like extension that bends behind, below and behind, the softpalate that holds the rigid tube or that it might not hold the tube, butsimply be a curved hollow ribbon that allows a device to be pushedbehind the soft palate, expanding as it leaves the tube. Or a bendabletube could be attached on a track alongside the ribbon-like extension,and could be pushed alongside and behind the soft palate.

The present disclosure provides a novel medical appliance for thetreatment of obstructive sleep apnea in a patient, the appliancecomprising: a securing device configured to be removably affixed to thepatient's jaw; and a biasing member which is insertable behind the softpalate and/or the base of the patient's tongue, thereby providing forthe flow of air in the nasopharyngeal airway; wherein the securingdevice is connected to the biasing member to allow insertion and/orremoval of the biasing member from the nasopharyngeal airway.

The appliance further comprising a connector device disposed between thesecuring device and the biasing member. The biasing member comprises atleast two concentric tubes, wherein a first concentric tube is disposedwithin a second concentric tube. The appliance further comprises a firstactuator which expands the biasing member by causing the firstconcentric tube to move in a vertical direction away from the secondconcentric tube. Alternatively, the appliance further comprises a thirdconcentric tube and a second actuator, wherein the first and secondactuators can be either the same actuator or different actuators.Preferably, the first concentric tube moves in an upward verticaldirection and the third concentric tube moves in a downward verticaldirections away from the second concentric tube. The first concentrictube is formed of a mesh wire. Optionally, the appliance furthercomprises a locking mechanism which prevents the first concentric tubefrom collapsing back within the second concentric tube.

Optionally, the biasing member comprises at least one tube having eithera circular or elliptical cross-section. The tube comprises a proximalend, a distal end and a lumen therethrough. Preferably, at least aportion of the tube comprises perforations to allow for air to passtherethrough. To provide structural integrity, the tube comprises atleast one or more rings disposed about a diameter of the tube, therebylimiting compression of the tube.

The appliance further comprises a release device for causing the biasingmember to unfold in a direction opposite to that of the biasing memberwhen inserted behind the soft palate and/or the base of the patient'stongue.

Preferably, the securing device is a palate retainer. The securingdevice is attached to either the upper or lower jaw of the patient. Thepalate retainer comprises a molded insert and at least one connectorused to connect the insert to the jaw. The connector is a wire securablymounted to at least one tooth of the jaw. Preferably, the molded insertis either continuous or non-continuous about the patient's palate.

The nasopharyngeal airway comprises a nasopharynx region and/or anoropharynx region.

Alternatively, the biasing member is at least one member selected fromthe group consisting of: a flexible or rigid stent, balloon, andcombination thereof. Preferably, the stent is housed in a tube orribbon, and further comprises an actuator to move the stent out of thehousing. The stent is typically formed from either a metal or magneticwire mesh. Optionally, at least one magnet can be disposed about thesecuring device and the biasing member is formed of a metal or othermagnetic material, such that the biasing member is attracted to themagnetic force of the magnet in the securing device (e.g., palateretainer) such that the biasing member is pulled toward the magnettogether with the soft palate or base of the tongue. Alternatively oradditionally, the biasing member may include a magnet, and the securingdevice includes a magnetic portion attracted to the biasing membermagnet.

Optionally, the biasing member expands either radially or longitudinallywhen in position behind the soft palate or base of the tongue. It ispreferably that the biasing member include an adjuster which operablyexpands or contracts the biasing member in either the radial orlongitudinal directions.

The connector device is removably disposed between the securing deviceand the biasing member. Preferably, the connector device is at least oneselected from the group consisting of: a ‘C’ shaped neck, collar orribbon, frictionally engaging surfaces, a snap fit assembly, a screwattached joint, hinged connector, and any combination thereto. Theconnector device applies a force to the biasing member to operablyadjust from a first magnitude to a second magnitude. Preferably,adjustment occurs over time or as at least a portion of the biasingmember transitions from a first temperature to a second temperature.

The hinged connector is preferably an adjustable force hinge. The hingedconnector further comprises a locking device which operably preventrotation of the hinged connector.

The appliance further comprises a force measurement assembly whichmeasures the force exerted by the biasing member upon the soft palate orthe base of tongue of the patient. The force measurement assembly is aforce transducer selected from the group consisting of: a strain gauge,a magnetic sensor, a capacitive sensor, a piezo transducer and acombination thereof.

The appliance further comprises a force monitor assembly which monitorsthe forces recorded by the force measurement assembly to determine isthe recorded force exceeds a threshold force.

The appliance further comprises a visualization assembly which providesan image of the area behind the soft palate and/or area behind the baseof the tongue. The visualization assembly is integral to the biasingmember, affixed to the securing device or an optical fiber which ispassed through the patient's nasal passage. The visualization assemblycomprising at least one fiber optic cable and at least one deviceselected from the group consisting of: a camera, a camera lens, and accd assembly.

A method for treating a patient having sleep apnea, the methodcomprising: inserting into a patient's mouth a medical appliance whichcomprises: a securing device configured to be removably affixed to thepatient's jaw; and a biasing member which is insertable behind the softpalate and/or the base of the patient's tongue, thereby providing forthe flow of air in the nasopharyngeal airway; wherein the securingdevice is connected to the biasing member to allow insertion and/orremoval of the biasing member from the nasopharyngeal airway. The methodfurther comprising: adjusting the size of the biasing member; adjustingthe force applied by the biasing member; and/or adjusting the positionof the biasing member relative to the securing device.

A method for diagnosing sleep apnea in a patient, the method comprising:inserting into a patient's mouth a medical appliance which comprises: asecuring device configured to be removably affixed to the patient's jaw;and a biasing member which is insertable behind the soft palate and/orthe base of the patient's tongue, thereby providing for the flow of airin the nasopharyngeal airway; wherein the securing device is connectedto the biasing member to allow insertion and/or removal of the biasingmember from the nasopharyngeal airway; and conducting at least onediagnostic procedure selected from the group consisting of: (a)measuring a force applied by the biasing member to the soft palate orbase of tongue of the patient; (b) viewing the amount of contact betweenthe biasing member and the soft palate or base of tongue of the patient;(c) inserting a visualization device into the mouth or nose of thepatient, wherein the visualization device is configured to visualize theamount of contact between the biasing member and the soft palate or baseof tongue of the patient; and (d) quantifying the size of the openingbetween the biasing member and the soft palate or base of the tongue ofthe patient.

A method of fabricating a medical application, the method comprising:producing a medical appliance which comprises: a securing deviceconfigured to be removably affixed to the patient's jaw; and a biasingmember which is insertable behind the soft palate and/or the base of thepatient's tongue, thereby providing for the flow of air in thenasopharyngeal airway; wherein the securing device is connected to thebiasing member to allow insertion and/or removal of the biasing memberfrom the nasopharyngeal airway; measuring a portion of a patient's oralcavity; and sizing the medical appliance to fit the measured oralcavity.

Further objects, features and advantages of the present disclosure willbe understood by reference to the following drawings and detaileddescription.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a cross-sectional view of a patient's soft palate, oral cavityand pharynx without any appliance disposed therein;

FIG. 2 is a schematic representation of a palate retainer with a tubeshaped nasopharyngeal extension having a ventilation hole disposedtherein, and a nasopharyngeal visualization system inserted through anostril of a patient, according the present disclosure;

FIG. 3 is a schematic representation of the tube shaped nasopharyngealextension of FIG. 2, wherein the tube expansible in both the upper andlower directions;

FIG. 4 is a schematic representation of the palate retainer with a tubeshaped nasopharyngeal extension disposed behind the soft palate, whereinthe palate retainer is secured to the teeth in the upper jaw to hold itin place;

FIG. 5 is a schematic representation of the palate retainer of FIG. 4,wherein the tube shaped nasopharyngeal extension is expanded in both theupper and lower directions;

FIG. 6 is a front perspective view of a palate retainer with aperforated tube shaped nasopharyngeal extension, wherein the retainerhas a retainer portion which is configured to come into contact with thesoft palate of a patient;

FIG. 6a is a front perspective view of a palate retainer with a solidtube shaped nasopharyngeal extension, wherein the retainer has aretainer portion which is configured to come into contact with the softpalate of a patient;

FIG. 7 is a front perspective view of a palate retainer with a tubeshaped nasopharyngeal extension, wherein the retainer has a retainerportion which is configured to be affixed to the upper jaw, but not comein contact with a substantial portion of the soft palate of a patient,wherein the tube shaped nasopharyngeal extension is secured to theretainer portion by means of a pair of curved ribbons, strap, conduits,etc.;

FIG. 7a is a front perspective view of a palate retainer with a tubeshaped nasopharyngeal extension, wherein the retainer has a retainerportion which is configured to be affixed to the upper jaw, but not comein contact with a substantial portion of the soft palate of a patient,wherein the tube shaped nasopharyngeal extension is secured to theretainer portion by means of a single curved ribbon, strap, conduit,etc.;

FIG. 7b (i) is yet another embodiment of the present disclosuredepicting a palate retainer, wherein the retainer has a retainer portionwhich is configured to be affixed to the upper jaw, but not come incontact with a substantial portion of the soft palate of a patient, andwherein a stent housing in the general shape of a curved or “C” shapedtube or ribbon for housing an expandable stent therein is disposed aboutat least one portion of the retainer portion;

FIG. 7b (ii) depicts the stent of FIG. 7b (i) wherein the stent is inthe exposed or expanded position, where, when attached to the upper jaw,the stent would expand upwards behind the soft palate from the tip ofthe curved hollow ribbon or tube; FIGS. 7b (iii)(a)-(d) are variousembodiments wherein the stent of FIG. 7b (i) is replaced with inflatableballoons or expandable wire balls;

FIG. 7b (iv) is another embodiment wherein the stent of FIG. 7b (i) isreplaced with a memory wire which forms a spiral or helicalconfiguration when exposed;

FIG. 7b (v) is another embodiment wherein the stent of FIG. 7b (i) isreplaced with a memory wire which forms a loop or ellipticalconfiguration when exposed;

FIG. 7c (i) is yet another embodiment of the present disclosuredepicting a the stent of FIG. 7b (i) wherein the stent is formed ofmetal or magnetic wire mesh and wherein at least one magnet is disposedabout the retainer portion (preferably after the metal or magnetic wiremesh is expanded from the hollow stent housing behind the soft palate),thereby allowing for the soft palate to be held in an opened positiondue to the magnetic force between the magnet on the retainer portion andthe wire mesh expanded behind the soft palate;

FIG. 7c (ii) depicts the stent of FIG. 7c (i) wherein the stent is inthe exposed or expanded position;

FIG. 7d is a cross-sectional view of an appliance according to thepresent disclosure according to another embodiment, wherein a palateretainer is a platform for both a fixed tube behind the soft palate anda downwardly expandable tube behind the base of a tongue, optionally,with an expansion bulb or the like;

FIG. 8 is a schematic representation of a side view of an applianceaccording the present disclosure, wherein an adjustable palate retaineris attached to adjustable upper and lower extensions, optionally with aforce transducer in communication with an electronic assembly,consistent with the present invention;

FIG. 9 is a front perspective view of an appliance according to thepresent disclosure, wherein a palate retainer is removably attachable toa collar portion which is attached to a tube shaped nasopharyngealextension, wherein the retainer includes two pivotally attached portionsand an electronic module in electronic communication with strain gaugesintegral to the nasopharyngeal extension;

FIG. 10A a schematic representation of a side view of an applianceaccording to the present disclosure, wherein an upper extension isrotatably attached to the palate retainer, maintained in a pre-deployedposition by a band;

FIG. 10B is a schematic representation of the side view of the applianceof FIG. 10A wherein the band has been removed and the upper extensionhas rotated into a deployed position;

FIG. 11 is a flow chart of a preferred method of diagnosing a patientsuspected of having sleep apnea using an appliance of the presentdisclosure; and

FIG. 12 is a flow chart of a preferred method of manufacturing anappliance of the present disclosure.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

The present disclosure can best be described by referring to thefigures, wherein FIG. 1 shows a cross-section of a patient's oral cavity1. Oral cavity 1 includes a tongue 3, upper jaw 5, lower jaw 7, softpalate 9, and epiglottis 11, as well as the nasopharynx region 13,oropharynx region 15 and laryngopharynx region 17.

FIG. 2 depicts system 200 which comprises visualization apparatus 180and appliance 100. Appliance 100 includes palate retainer 20 and a tubeshaped nasopharyngeal extension 24. Palate retainer 20 has beenpositioned about the upper jaw 5 and secured thereto via a wire or otherremovable securing device 22, such as a wire connected to the teeth.Affixed to retainer 20 by a neck or collar portion 21 is tube shapednasopharyngeal extension 24 which can be a solid tube with an airpassageway disposed thereto to allow air to flow from the nasalpassageway 26 through nasopharynx region 13 and into the oropharynxregion 15 and laryngopharynx region 17. Collar portion 21 may beconfigured to flex, such as via an integral hinge or flexible joint, toavoid applying excessive force to tissue such as when the patientswallows. Alternatively, tube shaped nasopharyngeal extension 24 can beformed of a wire mesh or other material which is capable of permittingair to flow therethrough, while splinting soft palate 9 and tongue 3,thereby preventing soft palate 9 and tongue 3 from falling back while atthe same time providing a rigid air passageway in the retopalatal andretrolingual space that cannot collapse. Extension 24 may include one ormore expanding members, such as an expandable cage or balloon,configured to apply a force to maintain patience of an airway of thepatient. System 200 further includes visualization apparatus 180comprising monitor 181 which is electronically attached to camera 182.Camera 182 attaches to fiberscope 185 at jack 183. The distal end offiberscope 185 includes lens 186, typically a fish eye or other end orside view lens configured to provide an image of the air passagewaysand/or inserted devices, such as an endoscopic camera commonly used invarious medical procedures. Visualization apparatus 180 can be used todiagnose or prognose a patient's sleep apnea, such as when an applianceof the present invention is inserted behind the soft palate and/or thebase of the patient's tongue. Alternatively or additionally,visualization apparatus 180 can be used to adjust one or more parametersof an appliance of the present invention, such as adjusting the size,geometry, exerted force, or other adjustable parameter of the appliance,described in detail herebelow. Alternatively or additionally,visualization apparatus 180 can be used to select from two or moredifferently configured appliances of the present invention, such as toselect an appliance of appropriate geometry for a specific patient, toprovide enhanced therapeutic benefit to that patient. In a system of thepresent invention, one appliance may have a first range ofadjustability, and a second appliance may have a second range ofadjustability different than the first.

FIG. 3 demonstrates an alternative embodiment of the present disclosurewherein tube shaped nasopharyngeal extension 24 may include either anupper (superior) extension 30 or lower (inferior) extension 32. Suchextensions 30, 32 can be gravity or spring actuated, and formed ofmaterials which allow for collapsing or bending, and for easy removalfrom oral cavity 1 after use. Preferably, upper extension 30 is formedof a perforated material, such as wire mesh with, optionally, reinforcedsections to prevent collapse, to all for air to flow therethrough.Alternatively, extension 30 can also be formed of a solid material,similar or identical to that of nasopharyngeal extension 24. Although,lower extension 32 is preferably formed of a solid material, it can alsobe formed of a perforated material similar to upper extension 30. Upperand lower extensions 30 and 32 have a construction including one or moreair flow channels, or are made of porous or perforated materials thatallow air to pass through. Having upper and lower extension (30, 32)protruding from nasopharyngeal extension 24 provides for reinforcementof the soft palate and tongue over a greater distance or length, andthereby prevents constriction between soft palate 9 and nasopharynxregion 13 and/or between tongue 3 and oropharynx region 15 due to sleepapnea conditions.

FIG. 4 is a schematic representation of a front planar view of oralcavity 1, wherein the upper jaw 5 and lower jaw 7 are spread apart toshow tongue 3, as well as the preferred positioning of palate retainer20 about the palate 40, such that tube shaped nasopharyngeal extension24 is disposed behind soft palate 9. FIG. 4 also shows wire or securingdevice 22 affixed to opposite sides of upper jaw 5 via securing wire 22about a respective tooth 42 a and 42 b on each side thereof. Securingwire 22 holds palate retainer 20 in place about palate 40 such thatnasopharyngeal extension 24 is securely positioned behind soft palate 9by means of a molded collar or neck 21 disposed between retainer 20 andextension 24 to maintain an air passageway between soft palate 9 andnasopharynx region 13 and oropharynx region 13 during sleep apneaattacks. Neck 21 may be configured to flex, such as via an integralhinge or flexible joint, to avoid applying excessive force to tissuesuch as when the patient swallows. 21

FIG. 5 is similar to FIG. 4, but demonstrates nasopharyngeal extension24 with upper and lower extensions 30 and 32, as shown in FIG. 3. Thisconfiguration is capable of permitting air to flow therethrough, whilesplinting soft palate 9 and tongue 3, thereby preventing soft palate 9and tongue 3 from falling back while at the same time providing a rigidair passageway in the retopalatal and retrolingual space that cannotcollapse.

FIGS. 6 and 6 a depict palate retainer 20 having a perforated and solidtube shaped nasopharyngeal extensions 50 and 52, respectively, connectedthereto by support 54 which resides in front and below the soft palate.In this embodiment, retainer 20 includes a continuous retainer portion56 which is disposed about the palate of the upper jaw, not shown.Extension 50 of FIG. 6 has a porous or perforated construction, whileextension 50 of FIG. 6a has a solid tube construction.

FIG. 7 is another embodiment according to the present disclosure,wherein a non-continuous retainer portion 58 is used in order to avoidsubstantial contact between the palate of the upper jaw and retainerportion 58, as well as the soft palate to avoid irritation or gaggingdue to such contact. Retainer portion 58 is secured to nasopharyngealextension 60 via a pair of oppositely disposed arched or “C” shapednecks or collars or ribbons 62, 64 or other securing devices which bendaround the sides of the soft palate to hold tube 60 behind the softpalate. Ribbons 62 and/or 64 may be configured to allow flexing betweenretainer 20 and extension 60, such as during swallowing.

FIG. 7a is a front perspective view of palate retainer 20 with tubeshaped nasopharyngeal extension 60, wherein retainer 20 has a retainerportion 58 which is configured to be affixed to the upper jaw, but notcome in contact with a substantial portion of the soft palate of apatient, wherein tube shaped nasopharyngeal extension 60 is secured tothe retainer portion by means of a single curved ribbon, strap, conduit,neck, collar, etc.61, preferably configured to flex during swallowing.

FIGS. 7b (i) and (ii) is yet another embodiment of the presentdisclosure depicting palate retainer 20, wherein retainer 20 hasretainer portion 58 which is configured to be affixed to the upper jaw(not shown), but not come in contact with a substantial portion of thesoft palate of a patient, and wherein a stent housing 71 in the generalshape of a tube or ribbon for housing expandable stent 73 therein isdisposed about at least one portion of retainer portion 58. FIG. 7b (ii)depicts stent 73 in the exposed or expanded position. In an alternativeembodiment, a second stent housing 71 is included, not shown butpreferably in a mirrored or symmetric configuration, on the oppositeside of palate retainer 20, and configured to exert a force on theopposite side of the soft palate of the patient.

Alternatively, the stent of FIG. 7b (i) can be replaced with theballoons of FIGS. 7b (iii)(a)-(d), wherein (a) and (b) show a pair ofballoons 201 or expandable wire balls that can be either inflated orexpanded by mechanical means, not shown. FIG. 7(b)(iii)(c) depicts apair of inflatable disks 203 encased in a wire mesh 205 according tostill yet another embodiment of the present disclosure. FIG.7(b)(iii)(d) is yet another embodiment wherein inflatable units 207 areencased in a wire mesh 209.

FIG. 7b (iv) is another embodiment wherein the stent of FIG. 7b (i) isreplaced with a memory wire 211 which forms a spiral or helicalconfiguration when exposed, such as when mechanically released or whenexposed to body temperature. Memory wire 211 may comprise a resilientlybiased material, such as Nitinol wire in a superelastic state or otherelastic metal, alloy or plastic. Alternatively, memory wire 211 maycomprise a shaped-memory material, such as a shaped memory alloy orshaped memory polymer.

FIG. 7b (v) is another embodiment wherein the stent of FIG. 7b (i) isreplaced with a memory wire 213, constructed of one or more materialsdescribed in reference to memory wire 211 of FIG. 7b (iv). Memory wire213 forms a loop or elliptical configuration when exposed, such as whenmechanically released or when exposed to body temperature.

FIGS. 7c (i) and (ii) is yet another embodiment of the presentdisclosure depicting stent housing 71 comprising stent 73 which ispreferably formed of a metal or magnetic wire mesh, and wherein at leastone magnet 75, comprising a corresponding magnet or magnetic material,is disposed about retainer portion 58, thereby allowing for the softpalate (not shown) to be held in an opened position due to the magneticforce between magnet 75 and the wire mesh stent 73 disposed in theexpanded position behind the soft palate. In an alternative embodiment,a second stent housing 71 is included, not shown but preferably in amirrored or symmetric configuration, on the opposite side of palateretainer 20, and configured to exert a force on the opposite side of thesoft palate of the patient. In another alternative embodiment, stenthousing 71 may be a simple wire or ribbon, without an internal stent,configured to exert a force on the soft palate. The wire or ribbon mayinclude one or more magnets or magnetic materials that exert a force onthe soft palate caused by their attraction force toward a correspondingmagnet or magnetic material disposed about retainer 20, disposed in aseparate component of the appliance, and/or implanted in the patient.The wire or ribbon may include one or more expandable assemblies, suchas one or more expandable balloons configured to exert a force on thesoft palate.

Alternatively or additionally, magnets or metal wire can be implantedwithin the soft palate, thereby utilizing magnetic forces to move thesoft palate toward magnet 75 to keep the soft palate from collapsinginto the airway of the patient.

FIG. 7d is yet another embodiment according to the present disclosureand depicts a cross-sectional view of an appliance 77, wherein palateretainer 20 is a platform for both a fixed tube 24 disposed behind softpalate 9 and a downwardly expandable tube 79 disposed behind the base ofa tongue 3, optionally, with a expansion bulb or the like (not shown butpreferably an expandable balloon or an expandable cage). In analternative embodiment, tube 79 is of ribbon or wire construction, suchas a nitinol ribbon or other elastically biased ribbon or wireconfigured to apply pressure behind the tongue of the patient. Fixedtube 24 and expandable tube 79 may be attached to retainer 20 such as toallow movement such as during patient swallowing.

Optionally, the nasopharyngeal extensions are formed of a compressedflexible tube with several hard plastic rings to prevent collapse of thetube.

FIG. 8 demonstrates an alternative embodiment of the appliance of thepresent disclosure wherein appliance 100′ includes adjustable palateretainer 120 which attaches to a palate extender device, adjustableupper extension 130. Upper extension 130 is adjustably attached to abase of tongue extender device, lower extension 140, which is alsoadjustable. Palate retainer 120 includes securing element 122,preferably two wire filaments, one on each side of the upper jaw,configured to be removably attached to the patient's upper teeth.Alternatively or additionally, appliance 100′ and the other appliancesof the present invention may be attached to the teeth of the lower jawof the patient. Palate retainer 120 further includes proximal portion120 a and distal portion 120 b which are adjustably attached viahorizontal adjustment means 123, such as a rack and pinion or othermechanical adjustment assembly. Adjustment means 123 can be adjusted,such as via a screwdriver or other tool, to adjust the overall length ofpalate retainer 120. Palate retainer 120 includes, on its distal end,collar portion 121 which flexibly and adjustably attaches to upperextension 130 via vertical adjustment means 124. Vertical adjustmentmeans includes rack 125 such that rotation of a screw of verticaladjustment means 124 causes vertical translation (e.g. rack and pinionsuperior and inferior adjustment) of upper extension 130 relative topalate retainer 120.

Upper extension 130 attaches to lower extension 140 via a verticallyadjustable assembly comprising upper arms 126 a and 126 b whichadjustably attach to lower arms 128 a and 128 b respectively. Adjustmentmeans 127 a adjustably connects upper arm 126 a to lower arm 128 a.Adjustment means 127 b adjustably connects upper arm 126 b to lower arm128 b. Adjustment means 127 a and 127 b each include a rotating screw orother means configured to move lower extension 140 toward or away fromupper extension 130.

Upper extension 130 may include means of adjusting its outer diameter,diameter adjustment means 132, such as a screwdriver or other toolactivated mechanism which causes radial expansion or contraction ofupper extension 130. Adjustment can be performed prior to, during, orafter placement of upper extension 130 behind the patient's softpalette. In a preferred embodiment, upper extension 130 is a wound coil,and activation of adjustment means 132 causes edge 131 to rotationallytranslate to increase or decrease the relative diameter of upperextension 130. Lower extension 140 may include means of adjusting itsouter diameter, diameter adjustment means 142, of similar or dissimilarconfiguration to adjustment means 132 of upper extension 130, butpreferably configured to be operably adjusted by a screwdriver or othertool to radially expand or contract lower extension 140, such as bytranslation of edge 141. Similarly, lower extension 140 may be adjustedprior to, during, or after placement behind the base of the tongue ofthe patient. In an alternative embodiment, upper extension 130 and/orlower extension 140 include one or more heat-activated components, suchas one or more Nitinol components configured to expand at bodytemperature, such that radial expansion occurs as upper extension 130and/or lower extension 140 transition from room temperature to bodytemperature (e.g. soon after placement in the patient's mouth).

Upper extension 130 may further include a sensor assembly, such asstrain gauge assembly 160, configured to provide information regardingone or more patient conditions or one or more conditions of upperextension 130. Strain gauge assembly 160 attaches to electronic module150 of palate retainer 120 via wire 161, typically a bundle of wiresand/or optical fibers which attaches to wire 151, also typically abundle of wires and/or optical fibers. Wire 151 is connected toelectronic module 150. Electronic module 150 may include power, such asbattery power, and signal storage and/or processing means, such as meansto store and/or process the information received from strain gaugeassembly 160. This information can be used to diagnose or prognose apatient's sleep apnea condition (e.g. the amount of force being appliedto upper extension 130, such as during sleep where higher closing forcemay correspond to more severe sleep apnea), and or optimize theadjustable parameters of one or more components of appliance 100′ (e.g.upper extension 130 diameter and/or vertical positioning). Electronicmodule 150 may include an electronic attachment port, jack 152, whichallows attachment of a handheld or other electronic device which candownload or upload information from or to electronic module 150.Alternatively or additionally, lower extension 140 may include a straingauge assembly, not shown but preferably electrically connected toelectronic module 150 or another electronic assembly.

Upper Extension 130 may further include a visualization element, lensassembly 170, a camera or camera lens assembly. Lens assembly 170attaches to electronic module 150 of palate retainer 120 via wire 171,typically a bundle of wires and/or optical fibers which is attached towire 151, also typically a bundle of wires and/or optical fibersattached to electronic module 150. Lens assembly 170 provides an imageof the inner surface of upper extension 130 and the tissue surroundingupper extension 130 (e.g. the soft palate), and can be used to diagnoseor prognose the patient's sleep apnea condition as well as adjust one ormore parameters of appliance 100′ such as the diameter of upperextension 130. Lens assembly 170 may be a CCD device used to recordimages, or may be a lens assembly in optical communication with aseparate CCD device such as a CCD device integral to electronic module150 or connected to electronic module 150 via jack 152. Alternatively oradditionally, lower extension 140 may include a camera or lens assembly,not shown but preferably electrically connected to electronic module 150or another electronic assembly.

FIG. 9 demonstrates an alternative embodiment of the appliance of thepresent disclosure wherein appliance 100″ includes a hinged palateretainer 120 which attaches to a palate extender device, upper extension130 via a detachable collar portion 121, which is configured to residein front and below (inferior to) the soft palate and flex such thatupper extension 130 can flex in relation to retainer 120. Palateretainer is configured for attachment to the teeth of the upper jaw, viasecuring elements 122, as has been described hereabove. Palate retainer120 includes receiving holes 134 a and 134 b which slidingly receiveprojecting pins 133 a and 133 b respectively, of collar portion 121,such that palate retainer 120 can be attached to collar portion 121after upper extension 130 is in place behind the patient's soft palate.In an alternative embodiment, appliance 100″ may include multipleassemblies including collar portion 121 and upper extension 130, eachconfigured to attach to a single palate retainer 120. Multiple sets ofupper extension 130 and collar portion 121 may be useful in diagnosingand/or treating a patient's sleep apnea, such as when each set is ofdifferent construction (e.g. diameters, biasing forces, and othergeometric and physical properties).

Palate retainer 120 includes two halved portions 120 a and 120 b whichare rotatably connected via hinges 129 a and 129 b. such that palateretainer 120 can be folded when collar portion 121 is not attached.Palate retainer 120 further includes electronic module 150 which iselectrically connected to wire 151, typically one or more wires and/orfiber optic cables. Wire 151 attaches to strain gauges 160 a and 160 bof upper extension 130. Forces recorded by strain gauges 160 a and 160 bare received and preferably recorded by electronic module 150, as hasbeen described above in reference to FIG. 8, to diagnose, prognose,and/or modify treatment of a patient having or suspected of having sleepapnea.

FIGS. 10A and 10B demonstrate an alternative embodiment of the applianceof the present disclosure wherein appliance 100′″ includes an adjustablelength palate retainer 120 which is rotatably attached to upperextension 130. Palate retainer 120 includes securing elements 122 (oneshown in side view but preferably one on each side) which attach palateretainer 120 to the teeth of the patient's upper jaw. Palate retainer120 includes, on its distal end, collar 121, which is configured toreside in front and below (inferior to) the soft palate of the patient.Collar 121 attaches to a palate extender device, upper extension 130 viaspring loaded hinge 135.

Referring specifically to FIG. 10A, upper extension 130 is biased in apre-deployed position by band 136 preferably of a rubber band or similarelastically biased construction connected the bottom portion of upperextension 130 to one or more securing elements 122, such as via one ormore hooks on upper extension 130 and/or securing elements 122, thatengage looped ends of band 136, hooks and loops not shown. In analternative embodiment, a gentle detachment or tearing force is appliedto remove band 136 from securing element 122 and/or upper extension 130.In the configuration of FIG. 10A, appliance 100′″ can be easily insertedinto the patient's mouth, and securing elements 122 attached to theteeth of the patient's upper jaw.

Once in place, band 136 can be detached from either or both securingelement 122 and upper extension 130, allowing upper extension 130 torotate to a position applying a biasing force to the patient's softpalate, in the configuration of FIG. 10A, patient's anatomy not shownbut described in detail hereabove. In a preferred method, band 136 isremoved from securing element 122 first, and slow manual translation ofthe band toward the back of the patient's throat causes a slowdeployment of upper extension 130 to be located behind and apply a forceto the soft palate of the patient. Once in place, band 136 can beremoved from upper extension 130 as has been described above.

FIG. 11 demonstrates a preferred method of diagnosing a patient known tohave or suspected of having sleep apnea. In Step 200, an appliance orsystem of the present invention is selected. The appliance selected mayinclude one or more diagnostic or sensing capabilities such as the forcemeasurement capabilities of an appliance of the present invention, suchas the appliances 100′ or 100″ of FIG. 8 or 9, respectively. Theappliance selected may be a system of the present invention, such assystem including two or more different appliances, or a system includinga visualization instrument, such as system 200 of FIG. 2, and anappliance of the present invention.

In Step 201, the appliance is inserted into the patient's mouth, and aextender device of the appliance is placed behind the soft palate and/orbehind the base of the patient's tongue. At this time, one or more otherdevices may be inserted into the patient, such as visualizationinstrument 180 of FIG. 2, or put in a position to monitor one or moreparameters of the patient, such as EEG or EKG electrodes, respirationmonitors, snoring monitors, sound monitors, and other physiologicmeasuring sensors and/or devices used to diagnose, prognose or otherwiseassess a sleep apnea patient.

In Step 202, the patient's breathing is assessed, such as by using theone or more diagnostic instruments described in reference to Step 201above. In a preferred embodiment, the assessment includes a period oftime when the patient is asleep. The assessment may include comparisonto similar testing performed without an appliance of the presentinvention in place in the patient, or with a differently configuredappliance used. The assessment phase may include adjusting one or moreparameters of the appliance, such as to modify the magnitude of abiasing force applied to the soft palate and/or the base of the tongue.The assessment may include a comfort assessment, such as comfortassessed through measurement of physiologic parameters or by completinga patient questionnaire.

FIG. 12 demonstrates a preferred method of manufacturing or adjusting anappliance of the present invention for a particular patient known tohave or suspected of having sleep apnea. In Step 300, a patientassessment is performed such as a diagnostic procedure performed whilethe patient is sleeping. The assessment may include the creation of oneor more images used to determine the proper dimensions of the appliance,such as images created with technologies such as x-ray, CT scan, Mill,ultrasound, and other imaging technologies commonly found in health carecenters. The imaging may be created by a camera, such as a camerainserted to the areas behind the patient's soft palate and tongue (e.g.imaging scopes entered through the nose and/or the mouth), whereinvisible light pictures are used to measure the patient's anatomy.

Step 301 includes the manufacture or adjustment of an appliance of thepresent invention based on the patient measurements performed and/orother data collected in Step 300. This manufacture of a new appliance,and/or adjustment of an existing appliance, allows patient-specifictreatment of a particular patient's sleep apnea and yields improvedcomfort for the patient (with an inserted device), as well as betterefficacy in treatment. Patient specific sizing of the extender devices(soft palate and/or base of tongue force exerting members) can becustomized to apply a sufficient force to maintain proper airflow,without applying unnecessary force. Extender device geometry can bechosen to apply force where beneficial, and avoid tissue contact that isunnecessary. Non-circular profiles, such as crescent profiles, can beused for extender devices to avoid contact with tissue to which no forceapplication is desired. This avoidance of skin contact can be particularimportant on the certain surfaces of the airways, such as some anteriorairway surfaces, on which swallowing and gag reflexes are mostsensitive.

While we have shown and described several embodiments in accordance withour invention, it is to be clearly understood that the same may besusceptible to numerous changes apparent to one skilled in the art.Therefore, we do not wish to be limited to the details shown anddescribed but intend to show all changes and modifications that comewithin the scope of the appended claims. In addition, each of thedrawings are not to scale, but are simply representative drawings toassist in the understanding of the present disclosure.

1. A medical appliance for a treatment of obstructive sleep apnea in apatient, said appliance comprising: a securing device configured to beremovably affixed to a jaw of the patient and extending through an oralcavity of the patient; a biasing member behind a soft palate of thepatient; and a connector device extending from one side of the securingdevice to the biasing member, wherein—the connector device houses thebiasing member, the biasing member comprising a portion that expands;wherein the one side of the securing device has a first radius ofcurvature with a first center of curvature below the securing device sothat the securing device is between the first center of curvature and abottom surface of the soft palate in the oral cavity for positioning inthe oral cavity and under the bottom surface of the soft palate, andwherein the connector device has a second radius of curvature with asecond center of curvature behind the soft palate so that the connectordevice is between the second center of curvature behind the soft palateand a nasopharynx region-of a nasopharyngeal airway behind the softpalate where the biasing member allows for a passage of air in thenasopharyngeal airway; wherein said biasing member exits from saidconnector device and said expandable portion expands behind saidpatient's soft palate to splint the soft palate of said patient toprovide the flow of air in a nasopharyngeal airway of the nasopharynxregion; and wherein said connector device connects said securing deviceto said biasing member to allow insertion and/or removal of said biasingmember into and/or from the nasopharyngeal airway.
 2. The medicalappliance according to claim 1, wherein the biasing member comprises astent.
 3. The medical appliance according to claim 1, wherein thebiasing member comprises a memory wire.
 4. The medical applianceaccording to claim 3, wherein the memory wire has a spiral or ellipticalshape when expanded.
 5. The medical appliance according to claim 1,wherein the biasing member is at least one member selected from thegroup consisting of: a flexible or rigid stent, a balloon, a memorywire, a tube, and a combination thereof.
 6. The medical applianceaccording to claim 5, wherein the connector device comprises a housingthat houses at least one of the flexible or rigid stent, the balloon,the memory wire, the tube, concentric tubes, and the combinationthereof.
 7. The medical appliance according to claim 1, wherein theconnector device is at least one selected from the group consisting of:a ‘C’ shaped neck, collar or ribbon, frictionally engaging surfaces, asnap fit assembly, a screw attached joint, hinged connector, and anycombinations thereof.
 8. The medical appliance according to claim 1,wherein the connector device is a wire securably mounted to at least onetooth of the jaw.
 9. The medical appliance according to claim 1, whereinthe connector device causes the biasing member to expand in a mannerselected from the group consisting of: adjusting a size of the biasingmember; adjusting a force applied by the biasing member; and/oradjusting a position of the biasing member relative to the securingdevice.
 10. The medical appliance according to claim 1, wherein thesecuring device is attached to either an upper or lower jaw of the jawof the patient.
 11. The medical appliance according to claim 1, furthercomprising a release device or adjuster for causing the biasing memberto exit from the housing or the expandable portion to expand wheninserted behind the soft palate and/or the base of a tongue of thepatient.
 12. The medical appliance according to claim 1, furthercomprising a nasopharyngeal extension that includes the biasing member,and that maintains an air passageway in the nasopharyngeal airway duringa sleep apnea attack.
 13. A medical appliance for a treatment ofobstructive sleep apnea in a patient, said appliance comprising: asecuring device configured to be removably affixed to a jaw of thepatient and extending through an oral cavity of the patient; anasopharyngeal extension that includes a biasing member behind a softpalate of the patient, and that maintains an air passageway in annasopharyngeal airway of the patient during a sleep apnea attack; and aconnector device extending from one side of the securing device to thebiasing member; wherein the one side of the securing device has a firstradius of curvature with a first center of curvature below the securingdevice so that the securing device is between the first center ofcurvature and a bottom surface of the soft palate in the oral cavity forpositioning in the oral cavity and under the bottom surface of the softpalate; wherein the connector device has a second radius of curvaturewith a second center of curvature behind the soft palate so that theconnector device is between the second center of curvature behind thesoft palate and the nasopharyngeal airway; and wherein said connectordevice connects said securing device to said biasing member to allowinsertion and/or removal of said biasing member into and/or from thenasopharyngeal airway.
 14. A method for diagnosing sleep apnea in apatient, said method comprising: inserting into a patient's mouth amedical appliance which comprises: a securing device configured to beremovably affixed to said patient's jaw; and a biasing member which isinsertable behind a soft palate and/or said a base of said patient'stongue, thereby providing for the flow of air in the nasopharyngealairway; wherein said securing device is connected to said biasing memberto allow insertion and/or removal of said biasing member from thenasopharyngeal airway; and conducting at least one diagnostic procedureselected from the group consisting of: (a) measuring a force applied bysaid biasing member to said soft palate or base of tongue of saidpatient; (b) viewing the amount of contact between said biasing memberand said soft palate or base of tongue of said patient; (c) inserting avisualization device into said mouth or nose of said patient, whereinsaid visualization device is configured to visualize the amount ofcontact between the biasing member and said soft palate or base oftongue of said patient; and (d) quantifying the size of the openingbetween said biasing member and said soft palate or base of the tongueof said patient.
 15. A method of fabricating a medical application, saidmethod comprising: producing a medical appliance which comprises: asecuring device configured to be removably affixed to said patient'sjaw; and a biasing member which is insertable behind the soft palateand/or the base of said patient's tongue, thereby providing for the flowof air in the nasopharyngeal airway; wherein said securing device isconnected to said biasing member to allow insertion and/or removal ofsaid biasing member from the nasopharyngeal airway; measuring a portionof a patient's oral cavity; and sizing said medical appliance to fitsaid measured oral cavity.